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2,3,4,5-tetrapropyl-cyclopenta-2,4-dienone | 105430-58-8

中文名称
——
中文别名
——
英文名称
2,3,4,5-tetrapropyl-cyclopenta-2,4-dienone
英文别名
2,3,4,5-tetrapropylcyclopentadienone;tetrapropylcyclopentadienone;cyclopentadienone;2,4-Cyclopentadien-1-one, 2,3,4,5-tetrapropyl-;2,3,4,5-tetrapropylcyclopenta-2,4-dien-1-one
2,3,4,5-tetrapropyl-cyclopenta-2,4-dienone化学式
CAS
105430-58-8
化学式
C17H28O
mdl
——
分子量
248.409
InChiKey
UREAXPPWHXVKLN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.3
  • 重原子数:
    18
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:4297c619d9bcfbe6886d9a308ad5e9eb
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反应信息

  • 作为产物:
    描述:
    甲苯 为溶剂, 以100%的产率得到2,3,4,5-tetrapropyl-cyclopenta-2,4-dienone
    参考文献:
    名称:
    CuCl-mediated tandem CO insertion and annulation of 1,4-dilithio-1,3-dienes: formation of multiply substituted cyclopentadienones and/or their head-to-head dimers
    摘要:
    在氯化铜的介导下,1,4-二硫-1,3-二烯与一氧化碳(CO)反应,通过串联 CO 插入和有机铜化合物的分子内/分子间环加成,生成多取代环戊二烯酮和/或其头对头二聚体。
    DOI:
    10.1039/b719007g
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文献信息

  • Reactions of Substituted (1,3-Butadiene-1,4-diyl)magnesium, 1,4-Bis(bromomagnesio)butadienes and 1,4-Dilithiobutadienes with Ketones, Aldehydes and PhNO To Yield Cyclopentadiene Derivatives and N-Ph Pyrroles by Cyclodialkenylation
    作者:Hongyun Fang、Guotao Li、Guoliang Mao、Zhenfeng Xi
    DOI:10.1002/chem.200400025
    日期:2004.7.19
    4-Dilithiobutadiene derivatives 1, 1,4-bis(bromomagnesio)butadiene derivatives 2 and metallacyclic (1,3-butadiene-1,4-diyl)magnesium reagents 3 were prepared and their reactions with ketones, aldehydes, and PhNO were investigated. Multiply substituted cyclopentadienes and N-Ph pyrroles were formed by unprecedented reaction conditions. The carbonyl group of aldehydes and ketones was deoxygenated during
    制备了1,4-二硫代丁二烯衍生物1,1,4-双(溴镁)丁二烯衍生物2和金属环(1,3-丁二烯-1,4-二基)镁试剂3,并与酮,醛和PhNO进行了反应调查。多重取代的环戊二烯和N-Ph吡咯是通过空前的反应条件形成的。醛和酮的羰基在​​反应过程中被脱氧,并在形式上表现为一碳单元;裂解PhNO的N == O部分,得到N-Ph吡咯衍生物。此外,揭示了这三种类型的试剂1、2和3之间的不同反应性。1,4-二锂试剂1容易与醛和酮反应;1,4-二镁试剂2与醛反应,但不与酮反应;
  • Nickel(O)-mediated hydrocyanation and carbonylation reactions of alkynes with trimethylsilyl(iso)cyanide
    作者:John J. Eisch、Allen A. Aradi、Kyoung I. Han
    DOI:10.1016/s0040-4039(00)81847-x
    日期:1983.1
    Under nickel(0) mediation, trimethylsilyl(iso)cyanide serves as both as useful -hydrocyanating agent and a carbohylating agent for alkynes.
    在镍(0)的介导下,三甲基甲硅烷基(异)氰化物既可用作有用的氢氰化剂,也可用作炔烃的碳氢化剂。
  • 1,1-Cycloaddition of Oxalyl Dichloride with Dialkenylmetal Compounds:  Formation of Cyclopentadienone Derivatives by the Reaction of 1,4,-Dilithio-1,3-dienes or Zirconacyclopentadienes with Oxalyl Chloride in the Presence of CuCl
    作者:Chao Chen、Chanjuan Xi、Yanfeng Jiang、Xiaoyin Hong
    DOI:10.1021/ja0506713
    日期:2005.6.1
    1,4-Dilithio-1,3-dienes or zirconacyclopentadienes reacted with oxalyl chloride in the presence of CuCl in a 1,1-cycloaddition manner to give cyclopentadienone derivatives in high yields along with the elimination of CO.
  • Garlaschelli, Luigi; Malatesta, Maria Carlotta; Panzeri, Silvia, Organometallics, 1987, vol. 6, # 1, p. 63 - 72
    作者:Garlaschelli, Luigi、Malatesta, Maria Carlotta、Panzeri, Silvia、Albinati, Alberto、Ganazzoli, Fabio
    DOI:——
    日期:——
  • Efficient Synthesis of Cyclopentadienone Derivatives by the Reaction of Carbon Dioxide with 1,4-Dilithio-1,3-dienes
    作者:Zhenfeng Xi、Qiuling Song
    DOI:10.1021/jo005641r
    日期:2000.12.1
    One-pot reaction of carbon dioxide with 1,4-dilithio-1,3-diene derivatives afforded cyclopentadienone derivatives bearing various substituents in high yields within several minutes.
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